chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113063001130630012CT36GENIChomozygous50715241
113063106930631070GA22GENIChomozygous50715242
113063152830631529CT43GENIChomozygous50715243
113063250630632507CG41GENIChomozygous50715244
113063329530633296GA36GENIChomozygous50715245
113063330630633307TC35GENIChomozygous50715246
113063369830633699AC48GENIChomozygous50715247
113063397230633976GTGT----3GENIChomozygous50715248
113063421430634215TC45GENIChomozygous50715249
113063465230634653AG48GENIChomozygous50715250
113063497230634973TC34GENIChomozygous50715251
113063559230635593CT58GENIChomozygous50715252
113063594130635942AC36GENIChomozygous50715253
113063655130636552AAAATTTTCTCT14GENIChomozygous50715254
113063671030636711TTCA47GENICpossibly homozygous50715255
113063704530637046GA35GENIChomozygous50715256
113063764130637642AG39GENIChomozygous50715257
113063796430637965CT53GENIChomozygous50715258
113063810830638109GA45GENIChomozygous50715259
113063859630638597AG53GENIChomozygous50715260
113063898630638987T-40GENICheterozygous50715261
113063898730638988GGAAAGAGCCAAACAAGGCCCTGCA42GENIChomozygous50715262
113063913930639140AG22GENIChomozygous50715263
113064009930640100AG49GENIChomozygous50715264
113064055830640559GA33GENIChomozygous50715265
113064068130640682AAT13GENIChomozygous50715266
113064079130640792CG46GENIChomozygous50715267
113064093630640937TTAACCACTGACTC30GENIChomozygous50715268
113064108030641081AAG9GENICheterozygous50715269
113064130830641318AATTGAGCTA----------4GENIChomozygous50715270
113064132330641324CT13GENICheterozygous50715271
113064161530641616TC53GENIChomozygous50715272
113064191330641914GC51GENIChomozygous50715273